D-Dimers are fibrin degradation products formed as a result of fibrinolysis or clot degradation by plasmin. Although plasmin cleaves fibrinogen, fibrin, and cross-linked fibrin during fibrinolysis, only the degradation of cross-linked fibrin, formed during active coagulation, results in D-Dimer formation. This fibrin-derived peptide can therefore be used as an effective biomarker to identify active coagulation and fibrinolysis.
The D-Dimer assay is now preferred in the evaluation and management of deep-vein thrombosis (DVT), a manifestation of thromboembolism, over conventional diagnostic tools due to its specificity and non-invasive nature.
As a biomarker, the D-Dimer assay provides critical diagnostic inputs to the clinician in the diagnosis and management of thromboembolism. Evaluation of D-Dimer levels is carried out in conjunction with the clinical probability of thromboembolism, as specified by Wells, et al. (2007).
Patients with high pre-test probability of thromboembolic disease should be tested for D-Dimer levels:
| Clinical Category | D-Dimer Test | Interpretation |
|---|---|---|
| Low-risk patients | Negative | Imaging tests can be avoided |
| Moderate-risk patients | Negative | Venous thromboembolism can be excluded No need for imaging |
The integration strategy of combining clinical assessment with the D-Dimer assay and imaging tests enable safer, more convenient, and cost-effective patient care by enabling: